PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white rod in a Tyvek polyethylene pouch, Rx Only, Manufactured by Teva Women's Health Inc. a subsidiary of Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 51285-204-01

This recall has been terminated (originally issued February 23, 2022).

Company

Coopersurgical, Inc

Recall Initiated

February 4, 2022

Posted

February 23, 2022

Recall Number

D-0643-2022

Voluntary / Mandated

Voluntary: Firm initiated

Quantity

48,645 cartons

Firm Location

North Tonawanda, NY, United States

Official Source

View on FDA website ↗